Forms a well-defined channel with 6 helices. Some paralogs tend to have an additional hydrophobic segment that might be a transit or signal peptide. It is unclear if the N-peptide is a signal or transit peptide. Localization: Mitochondrial (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005739 | mitochondrion | 5 | 3 |
GO:0020023 | kinetoplast | 2 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005743 | mitochondrial inner membrane | 5 | 13 |
GO:0016020 | membrane | 2 | 13 |
GO:0019866 | organelle inner membrane | 4 | 13 |
GO:0031090 | organelle membrane | 3 | 13 |
GO:0031966 | mitochondrial membrane | 4 | 13 |
Related structures:
AlphaFold database: E9AFS0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 16 |
GO:0006811 | monoatomic ion transport | 4 | 16 |
GO:0006817 | phosphate ion transport | 7 | 16 |
GO:0006820 | monoatomic anion transport | 5 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0015698 | inorganic anion transport | 6 | 16 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 16 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0055085 | transmembrane transport | 2 | 16 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 16 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 16 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 16 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 16 |
GO:1990547 | mitochondrial phosphate ion transmembrane transport | 4 | 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 16 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 16 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 16 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 16 |
GO:0022804 | active transmembrane transporter activity | 3 | 16 |
GO:0022857 | transmembrane transporter activity | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.426 |
DOC_AGCK_PIF_2 | 99 | 104 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 119 | 127 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 222 | 230 | PF00069 | 0.367 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.407 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.224 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.433 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.311 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.458 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.319 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.381 |
LIG_DLG_GKlike_1 | 58 | 66 | PF00625 | 0.458 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.429 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.407 |
LIG_LIR_Apic_2 | 9 | 15 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 107 | 113 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 134 | 144 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 270 | 281 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.303 |
LIG_PCNA_yPIPBox_3 | 71 | 85 | PF02747 | 0.390 |
LIG_Pex14_1 | 8 | 12 | PF04695 | 0.407 |
LIG_REV1ctd_RIR_1 | 197 | 207 | PF16727 | 0.306 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.440 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.298 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.395 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.396 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.319 |
LIG_SH2_GRB2like | 12 | 15 | PF00017 | 0.466 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 12 | 15 | PF00017 | 0.542 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.466 |
LIG_SH2_SRC | 209 | 212 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 91 | 94 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.344 |
LIG_SH3_1 | 12 | 18 | PF00018 | 0.442 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.442 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.368 |
LIG_SH3_4 | 215 | 222 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.371 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.511 |
MOD_CDC14_SPxK_1 | 55 | 58 | PF00782 | 0.318 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.389 |
MOD_CDK_SPxK_1 | 52 | 58 | PF00069 | 0.318 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.303 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.448 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.337 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.263 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.391 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.466 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.315 |
MOD_N-GLC_2 | 275 | 277 | PF02516 | 0.420 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.570 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.303 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.302 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.435 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.369 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.402 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.410 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.386 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.552 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.283 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.411 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.427 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.299 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.311 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.417 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I993 | Leptomonas seymouri | 84% | 100% |
A0A0S4JBC4 | Bodo saltans | 39% | 82% |
A0A0S4JNX4 | Bodo saltans | 72% | 94% |
A0A0S4KJX8 | Bodo saltans | 26% | 91% |
A0A1X0P0K9 | Trypanosomatidae | 39% | 100% |
A0A1X0P561 | Trypanosomatidae | 76% | 99% |
A0A3S5IRV4 | Trypanosoma rangeli | 77% | 100% |
A0A3S7X9V4 | Leishmania donovani | 99% | 100% |
A0A3S7X9Y0 | Leishmania donovani | 97% | 100% |
A0A422NF39 | Trypanosoma rangeli | 26% | 100% |
A4HNB1 | Leishmania braziliensis | 94% | 100% |
A4HNB2 | Leishmania braziliensis | 93% | 100% |
A4IBY2 | Leishmania infantum | 94% | 100% |
A4IBY3 | Leishmania infantum | 99% | 100% |
B0G143 | Dictyostelium discoideum | 25% | 100% |
C9ZYM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 100% |
D0A4I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 83% |
E9AFR9 | Leishmania major | 99% | 100% |
E9B6X2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
O04619 | Arabidopsis thaliana | 25% | 90% |
O61703 | Choristoneura fumiferana | 51% | 91% |
P12234 | Bos taurus | 51% | 88% |
P16036 | Rattus norvegicus | 50% | 89% |
P16260 | Homo sapiens | 25% | 95% |
P23641 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 100% |
P40035 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 44% | 100% |
P40614 | Caenorhabditis elegans | 56% | 93% |
Q00325 | Homo sapiens | 50% | 88% |
Q01888 | Bos taurus | 27% | 96% |
Q03829 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 86% |
Q29RM1 | Bos taurus | 25% | 100% |
Q54BF6 | Dictyostelium discoideum | 40% | 100% |
Q5R7W2 | Pongo abelii | 51% | 88% |
Q7DNC3 | Arabidopsis thaliana | 41% | 100% |
Q8C0K5 | Mus musculus | 25% | 95% |
Q8VEM8 | Mus musculus | 51% | 89% |
Q9FMU6 | Arabidopsis thaliana | 51% | 85% |
Q9M2Z8 | Arabidopsis thaliana | 49% | 87% |
Q9P7V8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
V5BT68 | Trypanosoma cruzi | 76% | 100% |